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Cognitive and Drug Therapy for Drug-Resistant Depression
This study has been completed.
First Received: November 2, 1999   Last Updated: December 6, 2005   History of Changes
Sponsor: National Institute of Mental Health (NIMH)
Information provided by: National Institute of Mental Health (NIMH)
ClinicalTrials.gov Identifier: NCT00000376
  Purpose

To develop an effective combined cognitive therapy (CT) plus drug treatment for patients with drug-resistant depression (DRD) (i.e., depression that is refractory to medication). To develop a manual for combined treatment for DRD that integrates three existing forms of CT (CT for depression, CT for personality disorders, and CT for anxiety disorders), and that specifies interventions for combining CT and medication when two therapists (psychotherapist and pharmacotherapist) provide the treatment. To obtain outpatient, randomized control, pilot data on the clinical value of the combined CT plus drug treatment, using the standard antidepressant desipramine (DMI), to obtain effect sizes and to determine if the treatment merits further investigation in a clinical trial. To develop a therapist adherence measure for the combined treatment.

Patients receive 1 of 2 treatments: CT plus DMI (n = 18) or DMI plus Clinical Management (n = 12). The first 6 of the 18 CT plus DMI patients are treated in a pre-pilot phase before randomization begins. All treatments continue for 6 months. The major assessment battery is administered at intake, 3 months, 6 months, and follow-up 6 months later. All treatments are closely monitored via audiotapes and supervision for purposes of developing and refining the CT plus drug treatment. The audiotapes are also used for development of the adherence measure. The primary outcome measures are Hamilton Rating Scale for Depression scores, Beck Depression Inventory scores, percent of patients who achieve clinical remission of symptoms, and percent showing attrition from treatment. Compliance with the treatment regimens is also a targeted and measured outcome variable.


Condition Intervention
Depression
Anxiety Disorders
Personality Disorders
Drug-Resistant Depression
Behavioral: Cognitive therapy
Drug: Desipramine

Study Type: Interventional
Study Design: Treatment, Randomized

Resource links provided by NLM:


Further study details as provided by National Institute of Mental Health (NIMH):

Study Start Date: March 1996
Estimated Study Completion Date: February 1999
Detailed Description:

To develop an effective combined cognitive therapy (CT) plus drug treatment for patients with drug-resistant depression (DRD) (i.e., depression that is refractory to medication). To develop a manual for combined treatment for DRD that integrates three existing forms of CT (CT for depression, CT for personality disorders, and CT for anxiety disorders), and that specifies interventions for combining CT and medication when two therapists (psychotherapist and pharmacotherapist) provide the treatment. To obtain outpatient, randomized control, pilot data on the clinical value of the combined CT plus drug treatment, using the standard antidepressant desipramine (DMI), to obtain effect sizes and to determine if the treatment merits further investigation in a clinical trial. To develop a therapist adherence measure for the combined treatment.

Patients receive 1 of 2 treatments: CT plus DMI (n = 18) or DMI plus Clinical Management (n = 12). The first 6 of the 18 CT plus DMI patients are treated in a pre-pilot phase before randomization begins. All treatments continue for 6 months. The major assessment battery is administered at intake, 3 months, 6 months, and follow-up 6 months later. All treatments are closely monitored via audiotapes and supervision for purposes of developing and refining the CT plus drug treatment. The audiotapes are also used for development of the adherence measure. The primary outcome measures are Hamilton Rating Scale for Depression scores, Beck Depression Inventory scores, percent of patients who achieve clinical remission of symptoms, and percent showing attrition from treatment. Compliance with the treatment regimens is also a targeted and measured outcome variable.

  Eligibility

Ages Eligible for Study:   21 Years to 60 Years
Genders Eligible for Study:   Both
Criteria

Inclusion Criteria:

-

Patients must have:

Drug-resistant depression (DRD).

  Contacts and Locations
Please refer to this study by its ClinicalTrials.gov identifier: NCT00000376

Sponsors and Collaborators
Investigators
Principal Investigator: Karla Moras, PhD
  More Information

No publications provided

Study ID Numbers: MH52737, DSIR
Study First Received: November 2, 1999
Last Updated: December 6, 2005
ClinicalTrials.gov Identifier: NCT00000376     History of Changes
Health Authority: United States: Federal Government

Keywords provided by National Institute of Mental Health (NIMH):
Adult
Antidepressive Agents, Tricyclic
Anxiety Disorders
Cognitive Therapy
Combined Modality Therapy
Depression
Desipramine
Female
Human
Male
Personality Disorders
Pilot Projects
Patient Care Team
Antidepressive Agents, Tricyclic -- *therapeutic use
Depression -- *therapy
Depression -- drug therapy
Desipramine -- *therapeutic use

Additional relevant MeSH terms:
Neurotransmitter Uptake Inhibitors
Neurotransmitter Agents
Depression
Disease
Adrenergic Agents
Molecular Mechanisms of Pharmacological Action
Adrenergic Uptake Inhibitors
Physiological Effects of Drugs
Psychotropic Drugs
Enzyme Inhibitors
Depressive Disorder
Desipramine
Pharmacologic Actions
Behavioral Symptoms
Antidepressive Agents, Tricyclic
Pathologic Processes
Anxiety Disorders
Mental Disorders
Therapeutic Uses
Mood Disorders
Central Nervous System Agents
Antidepressive Agents
Personality Disorders

ClinicalTrials.gov processed this record on November 09, 2009